Coexistence of pulmonary arterial hypertension and straight back syndrome in a patient with a novel BMPR2 variant affecting cytoplasmic tail domain

Background Pathologic variants in the bone morphogenetic protein receptor-2 (BMPR2) gene cause a pulmonary arterial hypertension phenotype in an autosomal-dominant pattern with incomplete penetrance. Straight back syndrome is one of the causes of pseudo-heart diseases. To date, no cases of idiopathic or heritable pulmonary arterial hypertension with straight back syndrome have been reported. Case presentation A 30-year-old female was diagnosed with pulmonary arterial hypertension by right heart catheterization. Computed tomography revealed a decreased anteroposterior thoracic space with heart compression, indicating a straight back syndrome. Genetic analysis by whole exome sequencing identified a novel c.2423_2424delGT (p.G808Gfs*4) germline frameshift variant within BMPR2 affecting the cytoplasmic tail domain. Conclusions This is the first report of different straight back characteristics in heritable pulmonary arterial hypertension with a novel germline BMPR2 variant. This finding may provide a new perspective on the variable penetrance of the pulmonary arterial hypertension phenotype. Supplementary Information The online version contains supplementary material available at 10.1186/s40001-024-01810-x.


Introduction
Pulmonary arterial hypertension (PAH), referring to group 1 pulmonary hypertension, is characterized by an unreversible increase in pulmonary vessel resistance (PVR) leading to right heart failure [1].The prevalence of PAH ranges from 48 to 55 cases per million adults in recent registries [2].Genetic heterogeneity, predominantly due to mutation in the bone morphogenetic protein receptor-2 (BMPR2) gene, is one of the most important associated factors for the etiologies of the disease [3].Approximately 85% of families with documented heritable PAH (HPAH) in one or more members carry a mutation in the BMPR2 gene.In sporadic PAH cases, 14-35% of patients, mostly in idiopathic PAH (IPAH), have an identified underlying pathogenic variant in BMPR2 [3].The structural change of PAH is demonstrated as an enlarged right heart with reduced function resulting from an irreversible elevation of PVR.Alterations of heart and great vessels' compression may occur in individuals with straight back syndrome due to an absence of normal physiological curvature of the dorsal spine [4].Here, we present a rare case of a PAH patient

Case presentation
A 30-year-old female was referred to our hospital in 2020 with a main complaint of intermittent dyspnea for five years, aggravated with syncope and exertional dyspnea for 6 months and exhibited a World Health Chest radiography showed prominent hilar pulmonary arteries, with a cardiothoracic ratio of 0.66 (Fig. 1A).Notably, the enlarged heart was compressed in a narrow anteroposterior thoracic space due to the straightening of the dorsal spine in the lateral view (Fig. 1B).Computed tomography (Fig. 1C-E) confirmed an enlargement of the right heart with a dilated main pulmonary artery of 30 mm in diameter.The ratio of the anteroposterior to the transverse chest diameter is 0.25, which is much smaller than normal.
An electrocardiogram disclosed signs of right axis deviation, right atrial and right ventricular enlargement (Fig. 1F).Transthoracic echocardiography showed that the right heart was dilated and the left ventricle was compressed (Fig. 1G).The tricuspid annular plane systolic excursion (TAPSE) was measured at only 12 mm and the right ventricular fractional area change (RV-FAC) was 26%, reflecting a reduced right heart systolic function.Right heart catheterization (Table 1) revealed severe precapillary pulmonary hypertension, with an elevated mPAP of 50 mmHg, pulmonary capillary wedge pressure (PAWP) of 8 mmHg, and PVR of 14.29 Wood units.An acute vasoreactivity testing was performed to show a negative response.Pulmonary artery angiogram indicated no evidence of pulmonary embolism or arteriovenous malformations.Blood tests revealed elevated levels of total bilirubin (38.9 µmol/l), direct bilirubin (11.4 µmol/l), and N-terminal pro-brain natriuretic peptide (NT-proBNP, 3020 pg/ml).Laboratory tests for autoimmune diseases and human immunodeficiency virus were all negative.The patient had no detectable associated medical agents known to cause PAH.Therefore, a genetic analysis by whole exome sequencing on a next generation sequencing approach was performed.A novel heterozygous frameshift germline variant in the exon 12 of the BMPR2 gene (c.2423_2424delGT,p.G808Gfs*4, NM_001204) was identified and subsequently validated (Fig. 2) by Sanger sequencing.The variant was absent in the Exome Sequencing Project, 1000 Genomes Project, or Exome Aggregation Consortium.This is a previously unreported variant, predicted to result in deleterious functional consequences.The deletion of two bases causes a frameshift alteration, which is defined as a null variant by the ACMG Standards and Guidelines [5], predicted premature protein truncation through nonsense-mediated decay.Hence, the patient was diagnosed with HPAH and straight back syndrome.
The patient was administrated sildenafil (25 mg three times daily) and bosentan (125 mg twice daily) therapy since 2016.As her symptoms worsened, the level of NT-proBNP was 3020 pg/ml with the dyspnea evaluated to be a WHO-FC III status on admission.Disease severity was evaluated as intermediate-high risk during this visit.The subsequent targeted therapy was escalated to a combination of sildenafil (25 mg three times daily), macitentan (10 mg once daily), and treprostinil injection (a gradual up-titration to 20 ng/kg/min).After six months, her   1).Her heart function remained to be WHO-FC II.The patient is currently comfortable with normal activities with no signs of symptomatically worsening, showing her benefits from triple combination therapy.

Conclusions and discussion
This is a rare case of HPAH with BMPR2 variant coexisting with straight back syndrome.BMPR2 encodes a type II receptor of the TGF-β family of signaling molecules, which participates in a multitude of cellular processes including pulmonary artery endothelial barrier function [6], smooth muscle cell proliferation, apoptosis and migration [7].Since the first BMPR2 mutation was identified in 2000, the use of advanced sequencing has allowed for the identification of more than ten validated disease-causing genes in PAH, mostly linked to the transforming growth factor beta (TGF-β)/SMAD pathway [8].However, not all BMPR2 mutation carriers will develop the disease during their lifetime due to a reduced penetrance.The penetrance of BMPR2 mutations is agedependent and has been estimated to be around 42% in women and 14% in men at most [9].Previous studies have reported that HPAH patients harboring BMPR2 mutations have an earlier onset of diagnosis and a severe disease prognosis with a short life span [10].The variant in this case is in the 12th exon of the BMPR2 gene, located in the cytoplasmic tail domain of the polypeptide (Fig. 2C and Additional file 1: Fig. S1A).According to the ACMG Standards and Guidelines [5], the variant is classified as pathogenic (Ib) based on evidence PVS1 (null variant in BMPR2), PM2 (absent from controls), and PM6 (assumed de novo, but without confirmation of paternity and maternity).Up to date, over 800 PAH-associated variants within BMPR2 have been reported, including more than 50% of all pathologic variants in the kinase domain and approximately 20% of them in the extended cytoplasmic tail domain (Additional file 1: Fig. S1B).Functional studies confirmed the loss of function in the BMP/SMAD pathway resulting from mutations affecting the kinase domain of BMPR2 [11].However, the effect of mutations in the cytoplasmic tail was able to retain most of its functions in SMAD signaling [12].Compared with the kinase domain, mutations in the cytoplasmic tail cause a milder phenotype with later disease onset and milder hemodynamic compromise at diagnosis, which is more similar to the disease profile in IPAH [11].In this case, the patient with a cytoplasmic tail BMPR2 variant may have a milder phenotype other than manifested with a relatively earlier onset at age 25.This indicates that additional modifying factors such as variants in untranslated regions or non-genetic factors might cause disease manifestation together, which is also called as "second-hit" model hypothesis in our previous report [13].
Straight back syndrome is a skeletal deformity by the loss of normal thoracic kyphosis.Since lacking the normal degree of dorsal curvature, the spine becomes vertical and a narrow space between the spine and the sternum which can be seen on the lateral chest X-ray [4].In this case, the ratio of anteroposterior to transthoracic diameter was 0.25, which was compatible with the criteria of straight back syndrome with a ratio of 1/3 or less [4,14].It occurs in thin individuals and is usually asymptomatic.Due to the proximity of the right heart to the anterior wall resulting from the forward and leftward shift of the right heart and main pulmonary artery, some have a cardiac murmur or an increased amplitude of the pulmonic sound resembling an atrial septal defect or other organic heart diseases [4].In this patient, the increase in the intensity of the pulmonic sound might be caused by both dilation and proximity of the main pulmonary artery.In a previous report, the absence of normal dorsal curvature of the spine was present in 9.2% of congenital heart disease [15].In addition, a reduced anteroposterior dimension of the thorax may cause asynchronous papillary muscle motion linked to mitral valve prolapse [16].The patient in this case was diagnosed with PAH, ruling out congenital heart defect, valve disorder or other vessel malformation screened by echocardiogram and pulmonary artery angiogram.Since the straight thoracic spine has not been previously reported in patients coexisting with IPAH or HPAH, so far it is not clear whether this skeletal abnormality has any correlation with the phenotypic features of PAH.However, the decreased sagittal diameter of the thoracic cage can result in a compressed heart, which might subsequently strengthen the load of pulmonary circulation.Therefore, this alteration may serve as an additional modifier to increase the penetrance of PAH disease manifestation in this BMPR2 variant carrier.
To our knowledge, this is the first report of a new variant in the cytoplasmic tail domain within BMPR2 leading to HPAH coexisting with a straight back syndrome, providing an explanation for the possible PAH phenotype manifestation.Our observation widens the BMPR2 variant landscape and strengthens the importance of a correct diagnosis of PAH.The diagnostic workflow with the molecular test should be more widely applied to allow for an earlier precision diagnosis and tailored interventions to delay the onset or treat PAH in the future.

Subjects and clinical characterization
Clinical data were collected including echocardiogram, X-ray computed tomography angiography, right heart catheterization and blood test.

DNA isolation
The EDTA-treated blood was collected from the peripheral blood of the patient.Genomic DNA was extracted using the Blood Genome Column Medium Extraction Kit (Kangweishiji, China), according to the manufacturer's recommendation.

Whole exome sequencing
The xGen Exome Research Panel v1.0 (IDT, Iowa, USA) includes 429,826 individually synthesized and quality-controlled probes, targeting 39 Mb coding region (19,396 genes) of the human genome and covers 51 Mb of end-to-end tiled probe space.Highthroughput sequencing was performed on the Illumina NovaSeq 6000 series sequencer (Illumina, San Diego, CA, USA).The sequencing process was performed by Chigene Translational Medicine Research Center (Beijing.China).More than 99% of targeted sequences were sequenced.Raw data were processed by Fastp software for adapters removing and filtering out low-quality reads (Q score of below 20).Sequencing reads passing quality filters were aligned to the Ensemble GRCh37/ hg19 reference genome using Burrows-Wheeler Aligner software.Single Nucleotide Polymorphisms (SNPs), short Indel calling and base quality score recalibration were conducted by Genome Analysis Toolkit software.After screening SNPs and Indels according to sequencing depth and high quality, reliable variants were obtained.

Variant analysis
The online system independently developed by Chigene (www.chige ne.org) was used to annotate databasebased minor allele frequencies (MAFs).The MAF < 0.1% in public databases (1,000 genomes, dbSNP, ESP, and ExAC database) was considered; Missense variants were analyzed by in silico tools (Provean, Sift, Pol-ypen2, Mutation Taster, M-Cap, and Revel) to predict protein product structure variation.As a prioritized pathogenicity annotation to ACMG guidelines, OMIM, HGMD and ClinVar databases were used as references of pathogenicity of every variant.

Sanger sequencing
The identified variant c.2423_2424delGT (p.G808Gfs*4) was further validated by Sanger sequencing using ABI 3730 sequencer (Applied Biosystems, Foster City, CA, USA).The origin of this newly identified variant might have been explored through the parents' DNA while the samples were not available.The primer sequences were designed as follows: Forward: 5′-CCG GCT AAA ATT TGG CAG CA-3′, Reverse: 5′-CCA GCT TGT TGC TCT CGT CT-3′.

Fig. 1
Fig. 1 Chest X-ray and CT scans of the patient.A Posteroanterior chest X-ray showing accentuation of vessels, prominence of pulmonary artery trunk and an enlarged heart shadow.B Lateral chest X-ray showing a straight curvature of the thoracic spine.C CT scan showing a dilated pulmonary artery and a narrow anteroposterior interval.D CT scan showing the heart is compressed in a narrow thoracic space with the right atrium adjacent to the posterior of the sternum.E CT scan showing a dilated right ventricle.F Electrocardiogram demonstrating a sinus rhythm with right axis deviation, and inverted T waves in lead II, III, aVF, V1-V4.G Echocardiogram showing of a dilated right ventricle and minimal pericardial effusion heart function was improved to WHO-FC II with an NT-proBNP level reduced to 352 pg/ml.Given her clinical improvement, a plan was made to transition from treprostinil injection to oral Selexipag up-titrated to 1.0 mg twice daily.No follow-up hemodynamic evaluation has been performed to date.The TAPSE was increased to 15 mm and the RV-FAC was of 29% by echocardiogram during the last follow-up on March 2023 (Table

Fig. 2
Fig. 2 Identification of the novel BMPR2 variant.A Family pedigree of the patient with PAH with straight back syndrome.The filled symbol represents the affected patients, empty circles/squares represent the unaffected members.The index patient (II 2) is indicated by a black arrow.B and C Sanger sequencing showing the variant of c.2423_2424delGT in the 12th exon within BMPR2, which is located in the cytoplasmic tail domain.ECD, extracellular domain; TMD, transmembrane domain; KD, kinase domain; CTD, cytoplasmic tail domain